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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403326Generated: October 30, 2026

Triethylamine → HCID 59729574, compound

https://huagongshe.com/reaction/403326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2,4-Dibenzyloxy-5-isopropyl-benzoic acidHCID 59167879—
Reactant1,3-Dimethyl-1H-indol-5-amineHCID 59550993—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59729574HCID 5972957495.3%

Reaction Steps

2,4-Dibenzyloxy-5-isopropylbenzoic acid (5.64 g, 15.0 mmol, 1.00 equiv.) in 80 mL dichloromethane at room temperature was treated with oxalyl chloride (2.00 g, 15.75 mmol, 1.05 equiv.) and catalytic amount of DMF (0.1 mL) for 1 hour. Solvent and excess (COCl)2 were removed on rotary evaporator. The residue was dissolved in 100 mL dichloromethane, and treated with 1,3-dimethyl-5-aminoindole (2.40 g, 15.0 mmol, 1.00 equiv.) and triethylamine (2.28 g, 22.5 mmol, 1.50 equiv.) at 0° C. for one hour. Normal aqueous workup and removal of solvent gave a light brown solid that was washed with ether to yield 2,4-dibenzyloxy-5-isopropyl-N-(1-methyl-1H-indol-5-yl)-benzamide (A) as off-white solid (7.20 g, 14.3 mmol, 95%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748424B2
Source datasetuspto-grants-2014_06
ORD IDord-3e48fbccac514504bf49d4e5e4bd0b09
Source noteuspto-grants-2014_06